Cannabinoid receptors in GtoPdb v.2025.1

Cannabinoid receptors (nomenclature as agreed by the NC-IUPHAR Subcommittee on Cannabinoid Receptors [127]) are activated by endogenous ligands that include N-arachidonoylethanolamine (anandamide), N-homo-γ-linolenoylethanolamine, N-docosatetra-7,10,13,16-enoylethanolamine and 2-arachidonoylglycerol. Potency determinations of endogenous agonists at these receptors are complicated by the possibility of differential susceptibility of endogenous ligands to enzymatic conversion [5].There are currently three licenced cannabinoid medicines each of which contains a compound that can activate CB1 and CB2 receptors [119]. Two of these medicines were developed to suppress nausea and vomiting produced by chemotherapy. These are nabilone (Cesamet®), a synthetic CB1/CB2 receptor agonist, and synthetic Δ9-tetrahydrocannabinol (Marinol®; dronabinol), which can also be used as an appetite stimulant. The third medicine, Sativex®, contains mainly Δ9-tetrahydrocannabinol and cannabidiol, both extracted from cannabis, and is used to treat multiple sclerosis and cancer pain.

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Publication Details

Journal
IUPHAR/BPS Guide to Pharmacology CITE
Published
2025-04-01
DOI
https://doi.org/10.2218/gtopdb/f13/2025.1
Citations
1
Primary Topic
Cannabis and Cannabinoid Research
Type
article
Field-Weighted Citation Impact
1.39
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article

Cannabinoid receptors in GtoPdb v.2025.1

Tom I. Bonner, Vincenzo Di Marzo, Christian C. Felder, A­llyn C. Howlett et al.
1 citations
IUPHAR/BPS Guide to Pharmacology CITE
Cannabis and Cannabinoid Research
1.39
article

Cannabinoid receptors in GtoPdb v.2025.1

Tom I. Bonner, Vincenzo Di Marzo, Christian C. Felder, A­llyn C. Howlett, Mary E. Abood, Peter J. Greasley, Ken Mackie, George Kunos, Roger G. Pertwee, Maurice R. Elphick, Francis Barth, Raphael Mechoulam, Ruth A. Ross, William A. Devane, Miles Herkenham, Ben Cravatt, Heather B. Bradshaw, S P H Alexander, Guy A. Cabral, Pierre Casellas
article en
1 citations

Abstract

Cannabinoid receptors (nomenclature as agreed by the NC-IUPHAR Subcommittee on Cannabinoid Receptors [127]) are activated by endogenous ligands that include N-arachidonoylethanolamine (anandamide), N-homo-γ-linolenoylethanolamine, N-docosatetra-7,10,13,16-enoylethanolamine and 2-arachidonoylglycerol. Potency determinations of endogenous agonists at these receptors are complicated by the possibility of differential susceptibility of endogenous ligands to enzymatic conversion [5].There are currently three licenced cannabinoid medicines each of which contains a compound that can activate CB1 and CB2 receptors [119]. Two of these medicines were developed to suppress nausea and vomiting produced by chemotherapy. These are nabilone (Cesamet®), a synthetic CB1/CB2 receptor agonist, and synthetic Δ9-tetrahydrocannabinol (Marinol®; dronabinol), which can also be used as an appetite stimulant. The third medicine, Sativex®, contains mainly Δ9-tetrahydrocannabinol and cannabidiol, both extracted from cannabis, and is used to treat multiple sclerosis and cancer pain.

IUPHAR/BPS Guide to Pharmacology CITEVol. 2025(1)
Hebrew College (US), North Carolina Central University (US), Scripps Research Institute (US), National Institutes of Health (US), University of Nottingham (GB), Queen Mary University of London (GB), Eli Lilly (United States) (US), University of Toronto (CA), University of Aberdeen (GB), Université de Montpellier (FR), University of Washington (US), Temple College (US), AstraZeneca (Brazil) (BR), Sanofi (Turkey) (TR), Indiana University (US), Virginia Commonwealth University Medical Center (US), Temple University (US)
Openalex Percentile: Top 22%
Cannabis and Cannabinoid Research
1.39
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